Canonical Allele Identifier: CA355962328
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002001C>G , CM000666.2:g.1002001C>G GRCh38
NC_000004.11:g.995789C>G , CM000666.1:g.995789C>G GRCh37
NC_000004.10:g.985789C>G NCBI36
NG_008103.1:g.20005C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.812C>G ENSP00000247933.4:p.Ser271Cys
ENST00000514224.2:c.812C>G MANE Select ENSP00000425081.2:p.Ser271Cys
ENST00000652070.1:n.868C>G
ENST00000247933.8:c.812C>G ENSP00000247933.4:p.Ser271Cys
ENST00000502910.5:c.671C>G ENSP00000422952.1:p.Ser224Cys
ENST00000514192.5:c.629C>G ENSP00000423685.1:p.Ser210Cys
ENST00000514224.1:c.416C>G ENSP00000425081.1:p.Ser139Cys
ENST00000514698.5:n.812C>G
NM_000203.4:c.812C>G NP_000194.2:p.Ser271Cys
NR_110313.1:n.900C>G
XM_006713882.2:c.416C>G XP_006713945.1:p.Ser139Cys
XM_011513459.1:c.771C>G XP_011511761.1:p.Leu257=
XM_011513460.1:c.671C>G XP_011511762.1:p.Ser224Cys
XM_011513461.1:c.605C>G XP_011511763.1:p.Ser202Cys
XM_011513462.1:c.524C>G XP_011511764.1:p.Ser175Cys
XM_011513463.1:c.524C>G XP_011511765.1:p.Ser175Cys
XR_924947.1:n.881C>G
NM_000203.5:c.812C>G MANE Select NP_000194.2:p.Ser271Cys
NM_001363576.1:c.416C>G NP_001350505.1:p.Ser139Cys
XM_011513461.2:c.605C>G XP_011511763.1:p.Ser202Cys
XM_017008163.1:c.-149C>G XP_016863652.1:n.-149C>G